Oligogenic heterozygosity in individuals with high-functioning autism spectrum disorders (Q35155976)

6 August 2017

title

Oligogenic heterozygosity in individuals with high-functioning autism spectrum disorders (English)

1 reference

6 August 2017

main subject

autism spectrum disorder

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autism

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high-functioning autism

1 reference

1 reference

Eric Boerwinkle

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Donna Muzny

object named as

Donna Muzny

0 references

Yasunari Sakai

0 references

Huda Y Zoghbi

0 references

Richard A Gibbs

1 reference

6 August 2017

Lora Lewis

1 reference

6 August 2017

Christian P Schaaf

1 reference

6 August 2017

Aniko Sabo

1 reference

6 August 2017

Jacy Crosby

1 reference

6 August 2017

Alicia Hawes

1 reference

6 August 2017

Humeira Akbar

1 reference

6 August 2017

Robin Varghese

1 reference

6 August 2017

publication date

30 May 2011

1 reference

6 August 2017

published in

Human Molecular Genetics

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6 August 2017

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6 August 2017

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6 August 2017

page(s)

3366-3375

1 reference

The Simons Simplex Collection: A Resource for Identification of Autism Genetic Risk Factors

6 August 2017

cites work

1 reference

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28 July 2018

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28 July 2018

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28 July 2018

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28 July 2018

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28 July 2018

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28 July 2018

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28 July 2018

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Linkage and association of the mitochondrial aspartate/glutamate carrier SLC25A12 gene with autism

28 July 2018

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No association between allelic variants of HOXA1/HOXB1 and autism

28 July 2018

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28 July 2018

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Association of INPP1, PIK3CG, and TSC2 gene variants with autistic disorder: implications for phosphatidylinositol signalling in autism

28 July 2018

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The HOXA1 A218G polymorphism and autism: lack of association in white and black patients from the South Carolina Autism Project

28 July 2018

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Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism

28 July 2018

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28 July 2018

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No association between HOXA1 and HOXB1 genes and autism spectrum disorders (ASD)

28 July 2018

1 reference

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No evidence for linkage of liability to autism to HOXA1 in a sample from the CPEA network

28 July 2018

1 reference

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FOXP2 is not a major susceptibility gene for autism or specific language impairment

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3153303

Lack of association between HoxA1 and HoxB1 gene variants and autism in 110 multiplex families

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3153303

Genetics of austim: complex aetiology for a heterogeneous disorder

28 July 2018

1 reference

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A forkhead-domain gene is mutated in a severe speech and language disorder

28 July 2018

1 reference

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Discovery of allelic variants of HOXA1 and HOXB1: genetic susceptibility to autism spectrum disorders

28 July 2018

1 reference

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28 July 2018

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Isolation of a Novel Human Homologue of the Gene Coding for Echinoderm Microtubule-Associated Protein (EMAP) from the Usher Syndrome Type 1a Locus at 14q32

28 July 2018

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Latent-class analysis of recurrence risks for complex phenotypes with selection and measurement error: a twin and family history study of autism

28 July 2018

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Epilepsy and the new cytogenetics

28 July 2018

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27 September 2018

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27 September 2018

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Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders

27 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3153303

CACNA1H mutations in autism spectrum disorders.

27 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3153303

Autistic behavior in children with fragile X syndrome: prevalence, stability, and the impact of FMRP.

27 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3153303

Subset of individuals with autism spectrum disorders and extreme macrocephaly associated with germline PTEN tumour suppressor gene mutations

27 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3153303

X-linked mental retardation and autism are associated with a mutation in the NLGN4 gene, a member of the neuroligin family

27 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3153303

Lack of association of HOXA1 and HOXB1 mutations and autism in Sicilian (Italian) patients

27 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3153303

Evaluation of FOXP2 as an autism susceptibility gene

27 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3153303

27 September 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDR243

21 January 2018

Identifiers

DOI

10.1093/HMG/DDR243

1 reference

6 August 2017

1 reference

6 August 2017

1 reference